3,5-Difluorobenzonitrile → 3-Fluoro-5-methoxybenzonitrile
Reaction equation
[CH3:1][O-:2].[Na+].[F:4][C:5]1[CH:6]=[C:7]([CH:10]=[C:11](F)[CH:12]=1)[C:8]#[N:9]>CO.CN(C)C=O.CCOCC>[F:4][C:5]1[CH:6]=[C:7]([CH:10]=[C:11]([O:2][CH3:1])[CH:12]=1)[C:8]#[N:9]Participants
6
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
Sodium methoxide (1.50 ml of a 4.5M solution in methanol, 7.10 mmol) was added dropwise to a stirred solution of 3,5-difluorobenzonitrile (1.00 g, 7.10 mmol) in N,N-dimethylformamide (36 ml) at 0° C. under nitrogen. The reaction was allowed to warm to room temperature and stirred for 14 hours. The reaction was diluted with ether (40 ml), washed with water (3×100 ml) and brine (100 ml), dried over magnesium sulphate, filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography on silica gel eluting with cyclohexane:ethyl acetate (95:5, by volume) to provide the title compound (418 mg) as a yellow oil.
Workup
- washwashed with water (3×100 ml) and brine (100 ml)
- dry with materialdried over magnesium sulphate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe crude product was purified by flash chromatography on silica gel eluting with cyclohexane:ethyl acetate (95:5, by volume)
Sources & evidence
- ORD record
- ord-051a0a0e5afd462e917fc459733eb5b0
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08063044B2
Reaction notes
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